Neurofibromatosis | search
Click here to view Neurofibromatosis news from 60+ newspapers.
Bookmark or Share- Neurofibromatosis type 1 - Diagnosis and treatment - Mayo ClinicTo diagnose neurofibromatosis type 1 (NF1), a healthcare professional begins with a review of your personal and family medical history and a physical exam. Your child's skin is checked for cafe au lait spots, which can help diagnose NF1.
- Neurofibroma - Symptoms and causes - Mayo ClinicA neurofibroma can arise with no known cause, or it may appear in people with a genetic condition called neurofibromatosis type 1. Neurofibromas most often are found in people ages 20 to 30 years old.
- Neurofibromatosis type 1 - Symptoms and causes - Mayo ClinicNeurofibromatosis type 1 (NF1) is a genetic condition that causes changes in skin pigment and tumors on nerve tissue. Skin changes include flat, light brown spots and freckles in the armpits and groin.
- Schwannomatosis - Symptoms and causes - Mayo ClinicNF2-related schwannomatosis was previously known as neurofibromatosis 2 (NF2). The other two types of schwannomatosis are SMARCB1-related schwannomatosis and LZTR1-related schwannomatosis. The altered genes that cause these types usually are not passed down through families.
- Neurofibromatosis tipo 1 - Síntomas y causas - Mayo ClinicLa neurofibromatosis tipo 1 (NF1) es una afección genética que causa cambios en la pigmentación de la piel y tumores en el tejido nervioso. Los cambios en la piel incluyen manchas sin relieve de color marrón claro y pecas en las axilas y en la ingle.
More
